rs1060503092

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1060503092(A;A)

Make rs1060503092(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

133264546

Gene

NDRG1

is a	snp
is	mentioned by
dbSNP	rs1060503092
dbSNP (classic)	rs1060503092
ClinGen	rs1060503092
ebi	rs1060503092
HLI	rs1060503092
Exac	rs1060503092
Gnomad	rs1060503092
Varsome	rs1060503092
LitVar	rs1060503092
Map	rs1060503092
PheGenI	rs1060503092
Biobank	rs1060503092
1000 genomes	rs1060503092
hgdp	rs1060503092
ensembl	rs1060503092
geneview	rs1060503092
scholar	rs1060503092
google	rs1060503092
pharmgkb	rs1060503092
gwascentral	rs1060503092
openSNP	rs1060503092
23andMe	rs1060503092
SNPshot	rs1060503092
SNPdbe	rs1060503092
MSV3d	rs1060503092
GWAS Ctlg	rs1060503092

Max Magnitude

0

ClinVar
Risk	rs1060503092(A;A)
Alt	rs1060503092(A;A)
Reference	Rs1060503092(G;G)
Significance	Probable-Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	NDRG1
CLNDBN	Charcot-Marie-Tooth disease, type IV
Reversed	1
HGVS	NC_000008.10:g.134276789C>T
CLNSRC
CLNACC	RCV000468626.1,